Department of Pharmaceutics, Faculty of Pharmacy, Alexandria University, Alexandria 21521, Egypt.
Department of Pharmaceutics, Faculty of Pharmacy, Alexandria University, Alexandria 21521, Egypt.
Biomed Pharmacother. 2022 Nov;155:113666. doi: 10.1016/j.biopha.2022.113666. Epub 2022 Sep 12.
Acute lung injury (ALI) and its more serious form; acute respiratory distress syndrome are major causes of COVID-19 related mortality. Finding new therapeutic targets for ALI is thus of great interest. This work aimed to prepare a biocompatible nanoformulation for effective pulmonary delivery of the herbal drug; tanshinone-IIA (TSIIA) for ALI management. A nanoemulsion (NE) formulation based on bioactive natural ingredients; rhamnolipid biosurfactant and tea-tree oil, was developed using a simple ultrasonication technique, optimized by varying oil concentration and surfactant:oil ratio. The selected TSIIA-NE formulation showed 105.7 nm diameter and a PDI ∼ 0.3. EE exceeded 98 % with biphasic sustained drug release and good stability over 3-months. In-vivo efficacy was evaluated in lipopolysaccharide (LPS)-induced ALI model. TSIIA-NE (30 µg/kg) was administered once intratracheally 2 h after LPS instillation. Evaluation was performed 7days post-treatment. Pulmonary function assessment, inflammatory, oxidative stress and glycocalyx shedding markers analysis in addition to histopathological examination of lung tissue were performed. When compared to untreated rats, in-vivo efficacy study demonstrated 1.4 and 1.9-fold increases in tidal volume and minute respiratory volume, respectively, with 32 % drop in wet/dry lung weight ratio and improved levels of arterial blood gases. Lung histopathology and biochemical analysis of different biomarkers in tissue homogenate and bronchoalveolar lavage fluid indicated that treatment may ameliorate LPS-induced ALI symptoms thorough anti-oxidative, anti-inflammatory effects and inhibition of glycocalyx degradation. TSIIA-NE efficacy was superior to free medication and blank-NE. The enhanced efficacy of TSIIA bioactive nanoemulsion significantly suggests the pharmacotherapeutic potential of bioactive TSIIA-NE as a promising nanoplatform for ALI.
急性肺损伤 (ALI) 及其更严重的形式——急性呼吸窘迫综合征是导致 COVID-19 相关死亡率的主要原因。因此,寻找治疗 ALI 的新靶点具有重要意义。本工作旨在制备一种生物相容性的纳米制剂,用于有效肺部递送达二氢丹参酮 I(TSIIA)治疗 ALI。采用简单的超声技术,基于生物活性天然成分——鼠李糖脂生物表面活性剂和茶树油,制备了纳米乳剂(NE)制剂,通过改变油浓度和表面活性剂:油的比例进行优化。选择的 TSIIA-NE 制剂显示出 105.7nm 的直径和 PDI∼0.3。EE 超过 98%,具有两相持续药物释放,在 3 个月内具有良好的稳定性。在脂多糖 (LPS) 诱导的 ALI 模型中评价了体内疗效。LPS 滴注后 2 小时,经气管内给予 TSIIA-NE(30μg/kg)一次。在治疗后 7 天进行评估。进行了肺功能评估、炎症、氧化应激和糖萼脱落标志物分析以及肺组织的组织病理学检查。与未治疗的大鼠相比,体内疗效研究表明,潮气量和分钟呼吸量分别增加了 1.4 倍和 1.9 倍,湿/干肺重比下降 32%,动脉血气水平得到改善。肺组织病理学和组织匀浆和支气管肺泡灌洗液中不同生物标志物的生化分析表明,治疗可能通过抗氧化、抗炎作用和抑制糖萼降解来改善 LPS 诱导的 ALI 症状。TSIIA-NE 的疗效优于游离药物和空白-NE。TSIIA 生物活性纳米乳剂的增强疗效显著表明了生物活性 TSIIA-NE 的治疗潜力,作为治疗 ALI 的有前途的纳米平台。